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OpenTrials
Completed

NCT Number: NCT01725464

The Effect of Nasal Cannula During the First 2 Hours Postoperative in Patient Undergoing Thoracotomy

During early postoperative after lung resection surgery, patients without oxygen supplementation may experience hypoxemia. Oxygen supplementation can be given via oxygen mask or cannular. In this study the investigators want to the sudy the effect of oxygen supplementation via oxygen cannular during the first 120 minutes after surgery

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Sirilak Suksompong

Bangkok, 10700, Thailand

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age =/> 18 years
  • lobectomy or pneumonectomy or wedge resection
  • ASA 1-3
  • preoperative oxygen saturation < 95 %
  • receiving epidural analgesia

Exclusion criteria

  • cannot communication

Treatment and study plan

oxygen cannular

Device

Patient receives oxygen supplementation 5 LPM via oxygen cannular for 120 minutes after the operative

Primary outcomes

  1. Mean oxygen saturation at 30 minutes postoperative

    Time frame: 30 minutes

Secondary outcomes

  1. incidence of oxygen saturation < 95% between 120 minutes until 3 days postoperative

    Time frame: 3 days

Sponsors and collaborators

Lead sponsor

Mahidol University

Other

Registry information

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Nov 12, 2012
Registry last updated
Aug 19, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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